Abstract
We report effects of SO2 and SO3 exposure on ammonium nitrate (AN) and N2O formation in Cu-CHA used for NH3-SCR. First-principles calculations and several characterizations (ICP, BET, XRD, UV-vis-DRS) were applied to characterize the Cu-CHA material and speciation of sulfur species. The first-principles calculations demonstrate that the SO2 exposure results in both (bi)sulfite and (bi)sulfate whereas the SO3 exposure yields only (bi)sulfate. Furthermore, SOx adsorption on framework-bound dicopper species is shown to be favored with respect to adsorption onto framework-bound monocopper species. Temperature-programmed reduction with H2 shows two clear reduction states and larger sulfur uptake for the SO3-exposed Cu-CHA compared to the SO2-exposed counterpart. Temperature-programmed desorption of formed ammonium nitrate (AN) highlights a significant decrease in nitrate storage due to sulfur species interacting with copper sites in the form of ammonium/copper (bi)bisulfite/sulfate. Especially, highly stable sulfur species from SO3 exposure influence the NO2-SCR chemistry by decreasing the N2O selectivity during NH3-SCR whereas an increased N2O selectivity was observed for the SO2-exposed Cu-CHA sample. This study provides fundamental insights into how SO2 and SO3 affect the N2O formation during ammonium nitrate decomposition in NH3-SCR applications, which is a very important topic for practical applications.
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